Testing Method for Specific Ingredients in Antiperspirant and Humectant Cosmetic Compositions

Total Page:16

File Type:pdf, Size:1020Kb

Testing Method for Specific Ingredients in Antiperspirant and Humectant Cosmetic Compositions (19) TZZ¥_¥_T (11) EP 3 156 793 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 19.04.2017 Bulletin 2017/16 G01N 31/22 (2006.01) (21) Application number: 15190253.3 (22) Date of filing: 16.10.2015 (84) Designated Contracting States: (72) Inventors: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB • TOMCZAK, Douglas Charles GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO Trumbull, Connecticut, 06611 (US) PL PT RO RS SE SI SK SM TR • AGRAWAL, Nikhil Designated Extension States: Trumbull, Connecticut, 06477 (US) BA ME • MARRIOTT, Robert Edward Designated Validation States: Bebington, Wirral, Merseyside, MA CH63 3JW (GB) • GIBSON, Oliver Lawrence (71) Applicants: Leeds, West Yorkshire, LS14 2AR (GB) • Unilever PLC London, Greater London EC4Y 0DY (GB) (74) Representative: McHugh, Paul Edward Designated Contracting States: Unilever PLC CY GB IE MT Unilever Patent Group • Unilever N.V. Colworth House 3013 AL Rotterdam (NL) Sharnbrook Designated Contracting States: Bedford AL AT BE BG CH CZ DE DK EE ES FI FR GR HR Bedfordshire MK44 1LQ (GB) HU IS IT LI LT LU LV MC MK NL NO PL PT RO RS SE SI SK SM TR (54) TESTING METHOD FOR SPECIFIC INGREDIENTS IN ANTIPERSPIRANT AND HUMECTANT COSMETIC COMPOSITIONS (57) A method of demonstrating the potential for a um-containingantiperspirant salt and/or moisturiser, said moisturisation and/or antiperspirancy effect from a cos- detector substance generating a visible colour change metic composition, said method comprising contacting to indicate the presence of aluminium-containing antiper- the composition with a detector substance for alumini- spirant salt and/or moisturiser. EP 3 156 793 A1 Printed by Jouve, 75001 PARIS (FR) 1 EP 3 156 793 A1 2 Description example, with reference to the following figures in which: [0001] The invention concerns a method for demon- FIGURE 1 is a photograph of three cosmetic com- strating the potential for a moisturisation and/or antiper- positions and a substrate prior to application, spirancy effect from a cosmetic composition. 5 [0002] Cosmetic compositions contain a number of dif- FIGURE 2 is a photograph of the three cosmetic ferent ingredients to perform various functions. Some compositions immediately after application to the cosmetic compositions are intended to provide a mois- substrate, turisation and/or antiperspirancy effect to the user. It is beneficial to be able to demonstrate the potential for a 10 FIGURE 3 is a photograph three minutes after ap- moisturisation and/or antiperspirancy effect from a cos- plication of the three cosmetic compositions to the metic composition. The present invention addresses that substrate, goal. [0003] According to the present invention, there is pro- FIGURE 4 is a photograph showing a positive result vided a method of demonstrating the potential for a mois- 15 from the application of a cosmetic composition to a turisation and/or antiperspirancy effect from a cosmetic test substrate, composition, said method comprising contacting the composition with a detector substance for aluminium- FIGURE 5 is a photograph of a negative result of the containing antiperspirant salt and/or moisturiser, said de- application of a comparative cosmetic product to a tector substance generating a visible colour change to 20 test substrate, indicate the presence of aluminium-containing antiper- spirant salt and/or moisturiser. FIGURE 6 is a photograph of PEG-8 applied to a [0004] Preferably, the moisturiser is a humectant. test substrate under ambient conditions, [0005] Conveniently, the step of contacting the com- position with the detector substance comprises the ap- 25 FIGURE 7 is a photograph of PEG-8 applied to a plication of the composition to a fibrous substrate com- test substrate within a desiccator, prising the detector substance. [0006] Advantageously, the fibrous substrate is paper. FIGURE 8 is a photograph showing the results of [0007] Preferably, the cosmetic composition is an an- the application of the surfactant Tween-20 and PEG- tiperspirant composition. 30 8, [0008] Advantageously, the cosmetic composition is in the form of a stick, aerosol, roll-on or cream. FIGURE 9 is a photograph showing the results of [0009] Preferably, the cosmetic composition is in the the application of two cosmetic compositions to a form of a stick test substrate with two different dilutions of a test [0010] Conveniently, the detector substance is for an 35 substance, and aluminium-containing antiperspirant salt. [0011] Advantageously, the detector substance com- FIGURE 10 is a photograph showing the results of prises Chromeazurol S or xylenol orange. the application of four cosmetic compositions to test [0012] Preferably, the detector substance is for a hu- substrates for the detection of glycerol and alumini- mectant. 40 um. [0013] Conveniently, the detector substance is for glycerol. [0019] Aluminium compounds are used in many cos- [0014] Advantageously, the detector substance com- metic compositions to provide antiperspirancy effects. It prises enzymes. would be beneficial to be able to demonstrate such an- [0015] Preferably, the detector substance is for poly- 45 tiperspirancy effects in a simple and quick way. In one propylene glycol or polyethylene glycol. aspect, the present invention relates to a method for dem- [0016] Conveniently, the detector substance compris- onstrating the potential for an antiperspirancy effect from es an inorganic salt and a pH indicator dye. a cosmetic composition comprising contacting the com- [0017] According to the invention, there is provided a position with a detector substance for aluminium contain- method of distinguishing a cosmetic composition having 50 ing antiperspirant salt, said detector substance generat- a moisturisation and/or antiperspirancy effect from an- ing a visible colour change to indicate the presence of other cosmetic composition, said method comprising an aluminium-containing antiperspirant salt. contacting the composition with a detector substance for [0020] To perform the method, the cosmetic composi- aluminium-containing antiperspirant salt and/or moistur- tion, which may for example be in the form of a stick, is iser, said detector substance generating a visible colour 55 contacted with the detector substance. This may be per- change to indicate the presence of aluminium-containing formed, for example, by mixing the composition with the antiperspirant salt and/or moisturiser. detector substance on a substrate surface, such as in a [0018] The invention will now be described, by way of container or vessel. Alternatively, the detector substance 2 3 EP 3 156 793 A1 4 may be present in or on a fibrous substrate, and the com- able from the Sigma Aldrich company. This particular re- position may be applied to the fibrous substrate. So, for agent contains a number of enzymes and other compo- example, the composition can be applied to the fibrous nents which can provide a visible colour change as an material, for example by applying a smear, and then the indication for the presence of glycerol in a test composi- substrate can be monitored to see whether there is a 5 tion. For this particular reagent, a colour change to purple colour change. indicates a positive result. [0021] Advantageously the method may, at least with [0027] In one aspect, a fibrous substrate can be used respect to the detection of moisturiser, be carried out in the test which may be, for example, paper or card. The ambient humidity conditions: in particular at relative hu- method can be used for compositions in the form of a midity of less than 80%, more particularly less than 70%. 10 stick and for compositions in non-stick forms, such as In one or more embodiments of particular interest the roll-on, aerosol or cream compositions. This is especially method is carried out at relative humidity of from 20 to the case for methods relating to humectants and antiper- 60%. spirant effects, particularly for glycerol and aluminium [0022] A test for the presence of aluminium can provide salts. a visible colour change to indicate the antiperspirancy 15 [0028] Other preferred moisturisers are triglycerides, potential of a product. A suitable test is the reagent such as those in sunflower seed oil. The present method Chromeazurol S obtainable from the Sigma Aldrich com- also relates to demonstrating the potential for moisturi- pany. For this particular reagent, a colour change from sation from cosmetic compositions containing such mois- orange to purple indicates a positive result. Another suit- turisers. A suitable detector substance is a reagent for able reagent is xylenol orange. 20 the presence of triglycerides. One such reagent is the [0023] Compounds such as some polypropylene gly- Serum Triglyceride Determination Kit available from the cols and polyethylene glycols are used in cosmetic com- Sigma Aldrich company. The kit contains enzymes and positions to provide moisturising properties. These par- other compounds. ticular materials are humectants. In other words, such [0029] The procedure involves enzymatic hydrolysis compounds help to retain moisture when applied to the 25 by lipase of the triglycerides to glycerol and free fatty skin of a user. The method relates to the demonstration acids. The glycerol produced is then measured by cou- of the presence of a range of moisturisers, inlcuding hu- pled enzyme reactions. mectants, such as polyethylene glycols, polypropylene [0030] Triglycerides are first hydrolyzed by lipoprotein glycols, butylene glycols, pentylene glycols, hexylene lipase to glycerol and free fatty acids. Glycerol is then glycols, isomers, dimers and trimers thereof, and other 30 phosphorylated by adenosine-5’-triphosphate (ATP) liquid "hydroxyl" humectants such as diglycerol and pol- forming glycerol-1-phosphate (G-1-P) and adenosine-5’- yglycerol. Preferably, the method involves the detection diphosphate (ADP) in the reaction catalyzed by glycerol of a polyethylene glycol, such as PEG-4, PEG-6, PEG- kinase (GK). G-1-P is then oxidized by glycerol phos- 8 and PEG-10.
Recommended publications
  • 1,3:2,4-Dibenzylidene-D-Sorbitol (DBS)
    This is a repository copy of 1,3:2,4-Dibenzylidene-d-sorbitol (DBS) and its derivatives- efficient, versatile and industrially-relevant low-molecular-weight gelators with over 100 years of history and a bright future. White Rose Research Online URL for this paper: https://eprints.whiterose.ac.uk/92625/ Version: Accepted Version Article: Okesola, Babatunde O., Vieira, Vânia M P, Cornwell, Daniel J. et al. (2 more authors) (2015) 1,3:2,4-Dibenzylidene-d-sorbitol (DBS) and its derivatives-efficient, versatile and industrially-relevant low-molecular-weight gelators with over 100 years of history and a bright future. Soft Matter. pp. 4768-4787. ISSN 1744-683X https://doi.org/10.1039/c5sm00845j Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ Please do not adjust margins Journal Name ARTICLE 1,3:2,4-Dibenzylidene-D-sorbitol (DBS) and its derivatives - Efficient, versatile and industrially-relevant low-molecular-weight Received 00th January 20xx, gelators with over 100 years of history and a bright future Accepted 00th January 20xx a a a a DOI: 10.1039/x0xx00000x Babatunde O.
    [Show full text]
  • Propylene Glycol TAP Report
    CFNP TAP Review Propylene glycol 2002 PROPYLENE GLYCOL Livestock Executive Summary Propylene glycol is a 3-carbon compound derived from propylene which has applications in both industry and medicine. The subject of the current petition is a request for the approval of propylene glycol to the National List for medical use in organic livestock. Propylene glycol is used as a drench in the treatment of ketosis. Propylene glycol is considered GRAS, except when used in or on cat food. Summary of TAP Reviewers’ Analyses1 Synthetic/ Allow without restrictions? Allow only with restrictions? Nonsynthetic (See Reviewers’ comments for restrictions) Synthetic (3) Yes (1) Yes (2) No (2) No (1) Identification Chemical names: 1,2-propanediol; 1,2-dihdroxypropane; Methyl glycol; Methylethylene glycol; Trimethyl glycol, C3H8O2; CH3CHOHCH2OH Other Names: 1,2-propylene glycol; 2-hydroxypropanol; alpha-Propylene glycol; alpha-propyleneglycol; Colla- Moist WS; Dowfrost; Horsechestnut HS; Methylethyl glycol; Methylethylene glycol; Monopropylene glycol; PG 12; Propane-1,2-diol; Propylene glycol; Propylene glycol USP; Sentry Propylene glycol; Sirlene; Solar winter ban; Uantox 20; Uantox 3; 1,2-proylenglykol [German] CAS Number: 57-55-6 Other numbers: EPA Pesticide Chemical Code: 068603 Chemical Structure: Characterization 1 This Technical Advisory Panel (TAP) review is based on the information available as of the date of this review. This review addresses the requirements of the Organic Foods Production Act to the best of the investigator’s ability, and has been reviewed by experts on the TAP. The substance is evaluated against the criteria found in section 2119(M) of the OFPA [7 USC 6517(m)]. The information and advice presented to the NOSB is based on the technical evaluation against that criteria, and does not incorporate commercial availability, socio-economic impact, or other factors that the NOSB and the USDA may want to consider in making decisions.
    [Show full text]
  • Polymeric Substances
    polymers.txt TOXIC SUBSTANCES CONTROL ACT INVENTORY REPRESENTATION FOR POLYMERIC SUBSTANCES I. Introduction This paper explains the conventions that are applied to listings of polymeric chemical substances for the Chemical Substance Inventory that is maintained by the U.S. Environmental Protection Agency (EPA) under the Toxic Substances Control Act (TSCA). These conventions have been in place largely without changes since the inception of the Inventory. The Agency's goal in developing this paper is to make it easier for the users of the Inventory to interpret listings for polymers and to understand how new substances should be identified for Inventory inclusion. Fundamental to the Inventory as a whole is the principle that entries on the Inventory are identified as precisely as possible for the commercial chemical substance, as reported by the submitter. Substances that are chemically indistinguishable, or even identical, may be listed differently on the Inventory, depending on the degree of knowledge that the submitters possess and report about such substances, as well as how submitters intend to represent the chemical identities to the Agency and to customers. Although these chemically indistinguishable substances are named differently on the Inventory, this is not a "nomenclature" issue, but an issue of substance representation. Submitters should be aware that their choice for substance representation plays an important role in the Agency's determination of how the substance will be listed on the Inventory. A. Polymer Definition For the purposes of the TSCA Inventory, a substance must meet the following compositional requirements in order to be considered a polymer: ===================================== NOTICE: The policies set out in this document are not final Agency action, but are intended solely as guidance.
    [Show full text]
  • Polyols, Propylene/Ethylene Oxide
    Report No. 46 POLYOLS FROM ETHYLENE OXIDE AND PROPYLENE OXIDE by YEN-CHEN YEN December 1968 A private report by the PROCESS ECONOMICS PROGRAM I STANFORD RESEARCH INSTITUTE MENLO PARK, CALIFORNIA I CONTENTS 1 INTRODUCTION, . , , . , . , , . , . , . , , . 1 2 SUMMARY . ,., ,, ,., , , , , , ,,,., , 3 3 INDUSTRY STATUS . , . , . , . 15 4 CHEMISTRY . , . , . 25 Oxyalkylation Reactions . , . 25 Catalysts . , . , . 27 Hydroxy1 Groups and Unsaturation . , . , 29 Kinetics...,..,..,.............. 31 Mechanism of Base-catalyzed Polyoxyalkylation . 33 Mechanism of Polyoxyalkylation with Boron-Trifluoride Catalyst . 37 Mechanism of Polyoxyalkylation Using Other Catalysts , , 38 Polymerization of Tetrahydrofuran . , , . 38 5 POLYGLYCOLS FROM ETHYLENE OXIDE AND PROPYLENE OXIDE , . 43 Review of Processes . , . , , . , , . 43 Reactors................ , . 47 Purification . , . , . , . , . 48 Manufacture of Polypropylene Glycol . , . , . 52 Process Description . , . , . , . , . , 52 Process Discussion , . , 57 Cost Estimate . , . , . , . 57 Manufacture of Polyethylene Glycol , . , . 64 Process Description . 64 Process Discussion . , . , . , . , . 68 Cost Estimate . , . , . , . 69 Other Polyglycols . , . , , , . , . , . 69 6 POLYOLS FROM POLYHYDRIC ALCOHOLS ............ 75 Review of Processes .................. 75 Control of Diol Content ............... 81 Dealing with Polyhydric Alcohols Having High Melting Points ....................... 81 Manufacture of Polyol from Glycerol and Propylene Oxide 82 Process Description ................. 82 Process Discussion
    [Show full text]
  • Chemical Compatibility Chart
    Chemical Compatibility Chart 1 Inorganic Acids 1 2 Organic acids X 2 3 Caustics X X 3 4 Amines & Alkanolamines X X 4 5 Halogenated Compounds X X X 5 6 Alcohols, Glycols & Glycol Ethers X 6 7 Aldehydes X X X X X 7 8 Ketone X X X X 8 9 Saturated Hydrocarbons 9 10 Aromatic Hydrocarbons X 10 11 Olefins X X 11 12 Petrolum Oils 12 13 Esters X X X 13 14 Monomers & Polymerizable Esters X X X X X X 14 15 Phenols X X X X 15 16 Alkylene Oxides X X X X X X X X 16 17 Cyanohydrins X X X X X X X 17 18 Nitriles X X X X X 18 19 Ammonia X X X X X X X X X 19 20 Halogens X X X X X X X X X X X X 20 21 Ethers X X X 21 22 Phosphorus, Elemental X X X X 22 23 Sulfur, Molten X X X X X X 23 24 Acid Anhydrides X X X X X X X X X X 24 X Represents Unsafe Combinations Represents Safe Combinations Group 1: Inorganic Acids Dichloropropane Chlorosulfonic acid Dichloropropene Hydrochloric acid (aqueous) Ethyl chloride Hydrofluoric acid (aqueous) Ethylene dibromide Hydrogen chloride (anhydrous) Ethylene dichloride Hydrogen fluoride (anhydrous) Methyl bromide Nitric acid Methyl chloride Oleum Methylene chloride Phosphoric acid Monochlorodifluoromethane Sulfuric acid Perchloroethylene Propylene dichloride Group 2: Organic Acids 1,2,4-Trichlorobenzene Acetic acid 1,1,1-Trichloroethane Butyric acid (n-) Trichloroethylene Formic acid Trichlorofluoromethane Propionic acid Rosin Oil Group 6: Alcohols, Glycols and Glycol Ethers Tall oil Allyl alcohol Amyl alcohol Group 3: Caustics 1,4-Butanediol Caustic potash solution Butyl alcohol (iso, n, sec, tert) Caustic soda solution Butylene
    [Show full text]
  • Polyalkylene Glycol Monobutyl Ether (PGME) for Handling
    Polyalkylene Glycol Monobutyl Ether (PGME) Handling/Processing 1 2 Identification of Petitioned Substance 3 19 Trade Names: 4 Chemical Names: 20 JEFFOX WL-660 (Huntsman) 5 Poly (ethylene glycol-ran-propylene glycol) 21 JEFFOX WL-5000 (Huntsman) 6 monobutyl ether 22 UCON ™ 50-HB-660 (Dow) 7 Other Name: 23 UCON™ 50-HB-3520 (Dow) 8 Polyethylene-propylene glycol, monobutyl ether 24 UCON™ HTF 14 (Aldrich) 9 Poly (ethylene glycol-co-propylene glycol) 25 Aldrich 438189 10 monobutyl ether 26 Teritol™ XD Surfactant 11 Oxirane, methyl-, polymer with oxirane, CAS Numbers: 12 monobutyl ether 9038-95-3 13 Oxirane, methyl-, polymer with oxirane, 14 monobutyl ether Other Codes: 15 PAGMBE MDL Number MFCD00198079 16 Propylene oxide ethylene oxide polymer PubChem Substance ID 248899946 17 monobutyl ether 18 27 28 Summary of Petitioned Use 29 30 The petitioner requests addition of polyalkylene glycol monobutyl ether (PGME) to the USDA National 31 Organic Program’s National List (7 CFR 205.605) as a non-agricultural substance. PGME is a polymeric 32 synthetic boiler additive with unique solubility properties (inverse solubility). It is used to improve boiler 33 steam quality. Steam is used as a conditioner for animal feed pellet production. The petitioner requests to 34 restrict the use of PGME products with molecular weight greater than 1500. 35 36 Characterization of Petitioned Substance 37 Composition of the Substance: 38 The substance is composed of high molecular weight (>1500) polymers of polyalkylene glycol monobutyl 39 ether, an aliphatic diether of polypropylene glycol. It is synthesized from butanol, propylene oxide and 40 ethylene oxide.
    [Show full text]
  • Methacrylated Poly(Ethylene Glycol)S As Precursors
    METHACRYLATED POLY(ETHYLENE GLYCOL)S AS PRECURSORS FOR SUPERPLASTICIZERS AND UV-CURABLE ELECTRICAL CONTACT STABILIZATION MATERIALS A Dissertation Presented to The Graduate Faculty of The University of Akron In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy Ali Javadi October, 2017 1 METHACRYLATED POLY(ETHYLENE GLYCOL)S AS PRECURSORS FOR SUPERPLASTICIZERS AND UV-CURABLE ELECTRICAL CONTACT STABILIZATION MATERIALS Ali Javadi Dissertation Approved: Accepted: Advisor Department Chair Dr. Mark D. Soucek Dr. Sadhan Jana Committee Member Dean of the College Dr. Sadhan Jana Dr. Eric J. Amis Committee Member Interim Dean of the Graduate School Dr. Miko Cakmak Dr. Chand Midha Committee Member Date Dr. Toshikazu Miyoshi Committee Member Dr. J. Richard Elliott ii ABSTRACT Poly(ethylene glycol)s (PEGs) are an important class of polymeric materials. In addition to standard linear PEGs, polymers synthesized from (meth)acrylated PEGs are specially versatile in modern technological applications. Comb-like copolymers derived from (meth)acrylated PEGs, such as polycarboxylate ethers (PCEs) are widely used as hydration and setting modifiers in cement while the working mechanisms in cement hydration have remained uncertain. The first part of this dissertation uncovers correlations between copolymer architecture and setting properties of cement for a range of synthesized PCEs architecture. Adsorption of PCEs on calcium silicate hydrate surfaces involves migration of Ca2+ ions in the acrylate backbone to the calcium silicate hydrate surface and subsequent ion pairing of the anionic polymer backbone with the positively charged surfaces of calcium-silicate-hydrate (C-S-H) gel. Two consistent sets of property correlations are identified as a function of copolymer design.
    [Show full text]
  • Equilibrium Limitations and Selectivity On
    EQUILIBRIUM LIMITATIONS AND SELECTIVITY ON CONVERSION OF GLYCEROL TO PROPYLENE GLYCOL ______________________________________________________ A Thesis presented to the Faculty of the Graduate School University of Missouri- Columbia ______________________________________________________ In Partial Fulfillment of the Requirements for the Degree Master of Science _______________________________________________________ by LIZANETTE RIVERA-RAMOS Dr. Galen J. Suppes, Thesis Supervisor AUGUST 2006 © Copyright by Lizanette Rivera-Ramos 2006 All Rights Reserved The undersigned, appointed by the Dean of the Graduate School, have examined the thesis entitled EQUILIBRIUM LIMITATIONS AND SELECTIVITY ON CONVERSION OF GLYCEROL TO PROPYLENE GLYCOL presented by Lizanette Rivera-Ramos a candidate for the degree of Master of Science and hereby certify that in their opinion it is worthy of acceptance. Dr. Galen J. Suppes Dr. Thomas R. Marrero Dr. Hsieh ACKNOWLEDGEMENTS I would like to express my sincere gratitude to my graduate advisor Dr. Galen Suppes, for his guidance, support, and contributions through my graduate studies. I would also like to thank Dr. Thomas R. Marrero for his comments and suggestions. Both of them had been excellent role models over the past years and I would like to thank them for giving me the opportunity to be their student. Appreciation is extended to Chuang-Wei “Roger” Chiu for provided me the guidance of an experienced researcher throughout my experimental work. Finally, I would like to thank the lab. team for their constant support
    [Show full text]
  • Polyethylene Glycol (Mean § 175.105 of This Chapter
    Food and Drug Administration, HHS § 178.3760 Substances Limitations Polybutene, hydrogenated (minimum viscosity at For use only: 99 °F, 39 Saybolt Universal seconds, as deter- 1. In polymeric substances used in contact with non-fatty food. mined by ASTM methods D445–82 (‘‘Standard 2. In polyethylene complying with § 177.1520 of this chapter and used in Test Method for Kinematic Viscosity of Trans- contact with fatty food, provided that the hydrogenated polybutene is parent and Opaque Liquids (and the Calculation added in an amount not to exceed 0.5 pct by weight of the polyethylene, of Dynamic Viscosity)’’) and D2161–82 (‘‘Stand- and further provided that such plasticized polyethylene shall not be used ard Method for Conversion of Kinematic Vis- as a component of articles intended for packing or holding food during cosity to Saybolt Universal Viscosity or to cooking. Saybolt Furol Viscosity’’), and bromine number 3. In polystyrene complying with § 177.1640 of this chapter and used in of 3 or less, as determined by ASTM method contact with fatty food, provided that the hydrogenated polybutene is D1492–78 (‘‘Standard Test Method for Bromine added in an amount not to exceed 5 pct by weight of the polystyrene, Index of Aromatic Hydrocarbons by Coulometric and further provided that such plasticized polystyrene shall not be used Titration’’), which are incorporated by reference. as a component of articles intended for packing or holding food during Copies may be obtained from the American So- cooking. ciety for Testing Materials, 100 Barr Harbor Dr., West Conshohocken, Philadelphia, PA 19428- 2959, or may be examined at the National Ar- chives and Records Administration (NARA).
    [Show full text]
  • Propylene Glycol Used As an Excipient
    9 October 2017 EMA/CHMP/334655/2013 Committee for Human Medicinal Products (CHMP) Propylene glycol used as an excipient Report published in support of the ‘Questions and answers on propylene glycol used as an excipient in medicinal products for human use’ (EMA/CHMP/704195/2013). 30 Churchill Place ● Canary Wharf ● London E14 5EU ● United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5555 Send a question via our website www.ema.europa.eu/contact An agency of the European Union © European Medicines Agency, 2017. Reproduction is authorised provided the source is acknowledged. Propylene glycol used as an excipient Table of contents Introduction ................................................................................................ 4 Scientific discussion .................................................................................... 5 1. Quality ..................................................................................................... 5 1.1. Physico-chemical properties ................................................................................... 5 1.2. Use in medicinal products ...................................................................................... 5 2. Pharmacokinetics .................................................................................... 6 2.1. Absorption ........................................................................................................... 6 2.1.1. Oral and IV pharmacokinetics.............................................................................
    [Show full text]
  • Physico-Chemical Properties of Polypropylene Glycols
    PHYSICO-CHEMICAL PROPERTIES OF POLYPROPYLENE GLYCOLS BY SALONI GUPTA [B.Sc. (Hons)] A thesis submitted in partial fulfilment of the requirements of the University of Greenwich for the Degree of Doctor of Philosophy January, 2015 Department of Chemical, Pharmaceutical & Environmental Sciences Faculty of Engineering & Science, University of Greenwich (Medway Campus), Chatham Maritime, Kent ME4 4TB, UK I DECLARATION I certify that this work has not been accepted in substance for any degree, and is not concurrently being submitted for any degree other than that of Doctor of Philosophy being studied at the University of Greenwich. I also declare that the work is the result of my own investigations except where otherwise identified by references and that I have not plagiarised the work of others. Saloni Gupta (Candidate): ………………................................................................................................................................. PhD Supervisors Dr A. P. Mendham: Prof. S. A. Leharne: Prof. B. Z. Chowdhry: Date: January 15th, 2015 II ACKNOWLEDGEMENTS I would like to express my sincere thanks to Prof. Stephen A. Leharne, Prof. Babur Z. Chowdhry and Dr Andrew P. Mendham for the invaluable guidance, support and encouragement they have given me as my supervisors throughout my PhD journey. They have always believed in me and encouraged me to do better. I am indebted to everyone who has assisted and encouraged me in the course of my studies, particularly Prof. Peter Griffiths, Dr Samuel Owusu-Ware, Dr Milan Antonijevic, Dr Beatrice Cattoz and Dr Joanna Thorne. The technical support I have received from staff members, particularly, Devyani, Atiya, Mark Allen, Steve Williams and the Link laboratory technicians has been invaluable. Most importantly thank you to my wonderful parents, my sisters (Sanya and Mannat) and my brother (Yatharth) for their love and encouragement.
    [Show full text]
  • Amended Safety Assessment of Butyl Polyoxyalkylene Ethers As Used in Cosmetics
    Amended Safety Assessment of Butyl Polyoxyalkylene Ethers as Used in Cosmetics Status: Final Amended Report Release Date: May 22, 2017 Panel Meeting Date: April 10-11, 2017 The 2017 Cosmetic Ingredient Review Expert Panel members are: Chairman, Wilma F. Bergfeld, M.D., F.A.C.P.; Donald V. Belsito, M.D.; Ronald A. Hill, Ph.D.; Curtis D. Klaassen, Ph.D.; Daniel C. Liebler, Ph.D.; James G. Marks, Jr., M.D.; Ronald C. Shank, Ph.D.; Thomas J. Slaga, Ph.D.; and Paul W. Snyder, D.V.M., Ph.D. The CIR Director is Lillian J. Gill, D.P.A. This safety assessment was prepared by Monice M. Fiume, Assistant Director/Senior Scientific Analyst/Writer and Bart Heldreth, Ph.D., Chemist. © Cosmetic Ingredient Review 1620 L Street, NW, Suite 1200 ♢ Washington, DC 20036-4702 ♢ ph 202.331.0651 ♢ fax 202.331.0088 ♢ [email protected] ABSTRACT The Cosmetic Ingredient Review (CIR) Expert Panel (Panel) assessed the safety of 46 butyl polyoxyalkylene ethers that share a common structural motif, namely a butyl chain (4 carbon alkyl chain) bound to a polyoxyalkylene (PPG, PEG, or both); 23 of these ethers were previously reviewed by the Panel, and 23 are reviewed for the first time. Most of the butyl polyoxyalkylene ethers have several functions in cosmetics, but the most common functions include hair conditioning agent and skin conditioning agent, and many function as solvents. Upon review of new data, including frequency and concentration of use, and data from previous CIR reports and on read-across analogs, the Panel concluded that these ingredients are safe in the present practices of use and concentration in cosmetics when formulated to be non-irritating.
    [Show full text]